Diagnostic Ultrasound System - FDA Registration 403baa3157da1cf9afc88614c6e56d70
Access comprehensive regulatory information for Diagnostic Ultrasound System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 403baa3157da1cf9afc88614c6e56d70 and manufactured by Siemens Healthineers Ltd. The device was registered on July 20, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
403baa3157da1cf9afc88614c6e56d70
Diagnostic Ultrasound System
FDA ID: 403baa3157da1cf9afc88614c6e56d70
Device Classification
Brand Name
Siemens
Registration Information
Analysis ID
403baa3157da1cf9afc88614c6e56d70
Registration Date
July 20, 2022
Manufacturer
Authorized Representative

